Canonical Allele Identifier: CA2260086846
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586485A= , CM000679.2:g.41586485A= GRCh38
NC_000017.10:g.39742737A= , CM000679.1:g.39742737A= GRCh37
NC_000017.9:g.36996263A= NCBI36
NG_008624.1:g.5411T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.350T= MANE Select ENSP00000167586.6:p.Val117=
ENST00000167586.6:c.350T= ENSP00000167586.6:p.Val117=
NM_000526.4:c.350T= NP_000517.2:p.Val117=
NM_000526.5:c.350T= MANE Select NP_000517.3:p.Val117=